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Q.Write notes on

(a) Wurtz reaction
(b) Corey-House alkane synthesis
(c) Huckel's rule OR How will you prepare the following compounds from benzene?
(a) Chlorobenzene
(b) Nitrobenzene
(c) Toluene
(d) Benzene Sulphonic Acid. Give the mechanism of nitration of benzene.
Jammu Kashmir JkboseJammu and Kashmir Board of School Education (Class 11) 2026Subjective· 5mImportance★★★★★
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Wurtz reaction and Corey-House synthesis are two methods to build higher alkanes from alkyl halides (Corey-House being cleaner for unsymmetrical products), and Huckel's rule is the pi-electron-counting criterion (4n+2 vs 4n) for aromaticity.

  1. Wurtz reaction: 2 R-X + 2 Na --(dry ether)--> R-R + 2 NaX Two molecules of an alkyl halide are treated with sodium metal in dry ether; the sodium removes the halogen atoms and couples the two alkyl groups together, forming a higher alkane with (in the simplest case, using one alkyl halide) an even number of carbon atoms. It is a useful method for preparing symmetrical alkanes, but is unsuitable for unsymmetrical or odd-carbon alkanes because mixing two different alkyl halides gives an inseparable mixture of three coupling products (see item 28).
  2. Corey-House alkane synthesis: This is a more controlled, three-step method for making unsymmetrical alkanes cleanly:
  1. An alkyl halide reacts with lithium metal in dry ether to form an alkyllithium: R-X + 2Li -> R-Li + LiX
  2. Two equivalents of the alkyllithium react with cuprous iodide (CuI) to form lithium dialkyl cuprate (also called a Gilman reagent): 2 R-Li + CuI -> R2CuLi + LiI
  3. The lithium dialkyl cuprate is then treated with a second, different alkyl halide (R'-X); only one of the two R groups couples with R', giving the unsymmetrical alkane cleanly: R2CuLi + R'-X -> R-R' + R-Cu + LiX

Because the coupling in the final step proceeds cleanly (unlike the mixture problem in Wurtz reaction), Corey-House synthesis is the preferred method for preparing unsymmetrical alkanes, including those with an odd total number of carbons.

(c) Huckel's rule:

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